NDC 52904-468

Pain Relief Maximum Strength

Acetaminophen,aspirin,caffeine

Pain Relief Maximum Strength is a Oral Tablet, Coated in the Human Otc Drug category. It is labeled and distributed by Select Corporation. The primary component is Acetaminophen; Aspirin; Caffeine.

• Product ID: 52904-468_f2f10382-7393-4c08-848a-6cbb96187e8a
• NDC: 52904-468
• Product Type: Human Otc Drug
• Proprietary Name: Pain Relief Maximum Strength
• Generic Name: Acetaminophen,aspirin,caffeine
• Dosage Form: Tablet, Coated
• Route of Administration: ORAL
• Marketing Start Date: 2012-10-15
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Labeler Name: Select Corporation
• Substance Name: ACETAMINOPHEN; ASPIRIN; CAFFEINE
• Active Ingredient Strength: 250 mg/1; mg/1; mg/1
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 52904-468-02

2 TABLET, COATED in 1 PACKET (52904-468-02)

• Marketing Start Date: 2012-10-15
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 52904-468-02 [52904046802]

Pain Relief Maximum Strength TABLET, COATED

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-10-15
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
ACETAMINOPHEN	250 mg/1

OpenFDA Data

• SPL SET ID: d60dcb6c-05ac-4ed0-a572-b84de75faeff
• Manufacturer:
  • Select Corporation
• UNII:
  • 362O9ITL9D
  • R16CO5Y76E
  • 3G6A5W338E
• RxNorm Concept Unique ID - RxCUI:
  • 308297
• Pharm Class PE:
  • Decreased Prostaglandin Production [PE]
  • Decreased Platelet Aggregation [PE]
• PHarm Class EPC:
  • Nonsteroidal Anti-inflammatory Drug [EPC]
  • Platelet Aggregation Inhibitor [EPC]
• NUI Code:
  • N0000008832
  • N0000008836
  • N0000175721
  • N0000000160
  • N0000175578
  • N0000175722